PREGABALIN LAPL pregabalin 50 mg capsule blister pack

Nchi: Australia

Lugha: Kiingereza

Chanzo: Department of Health (Therapeutic Goods Administration)

Viambatanisho vya kazi:

pregabalin, Quantity: 50 mg

Inapatikana kutoka:

Lupin Australia Pty Limited

INN (Jina la Kimataifa):

Pregabalin

Dawa fomu:

Capsule, hard

Tungo:

Excipient Ingredients: pregelatinised maize starch; purified talc; titanium dioxide; purified water; Gelatin; sodium lauryl sulfate; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; Shellac; strong ammonia solution; iron oxide black; potassium hydroxide; ethanol absolute

Njia ya uendeshaji:

Oral

Vitengo katika mfuko:

20, 14, 56, 60

Dawa ya aina:

(S4) Prescription Only Medicine

Matibabu dalili:

Pregabalin LAPL is indicated for the treatment of neuropathic pain in adults. Pregabalin LAPL is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Bidhaa muhtasari:

Visual Identification: Size '4' capsules with white cap and white body, imprinted with "PG" on the cap and with a band and with "50" on the body in black ink, containing white to off white powder; Container Type: Blister Pack; Container Material: PVC/Al; Container Life Time: 24 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Neither child resistant closure nor restricted flow insert

Idhini hali ya:

Licence status A

Idhini ya tarehe:

2014-12-05